TRABD2B (UniProt ID: A6NFA1), also known as TIKI2, is a metalloprotease that cleaves specific Wnt proteins (e.g., WNT3A, WNT5) to inhibit Wnt signaling, a pathway critical for embryonic development and tissue homeostasis . The biotin-conjugated TRABD2B antibody facilitates targeted detection in assays such as ELISA, immunohistochemistry (IHC), and western blot (WB) .
The antibody targets residues 195–405 of TRABD2B, a region critical for its metalloprotease activity . Cross-reactivity is confirmed exclusively in human samples, with no reported reactivity in other species . The biotin conjugation method (likely ZBPA-based, as per general best practices ) ensures specificity without nonspecific binding to albumin or other proteins .
ELISA: Direct antigen capture in sandwich assays, with detection via streptavidin-HRP conjugates .
Western Blot: Detects TRABD2B at ~65–79 kDa in human cell lines (DU 145, HT-29, HeLa) .
Immunohistochemistry: Potential for tissue-specific localization studies, pending protocol optimization .
Western Blot: Strong bands observed at 65–79 kDa in DU 145 (prostate cancer), HT-29 (colon cancer), and HeLa (cervical cancer) cells, confirming specificity .
IHC Compatibility: Biotinylation methods like ZBPA minimize background staining compared to non-specific conjugation techniques (e.g., Lightning-Link) .